Variant report
Variant | rs10124464 |
---|---|
Chromosome Location | chr9:79039091-79039092 |
allele | A/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr9:79034800-79046000 | Weak transcription | ES-I3 Cell Line | embryonic stem cell |
2 | chr9:79036800-79039200 | Weak transcription | Primary T cells effector/memory enriched fromperipheralblood | blood |
3 | chr9:79037400-79039400 | Enhancers | Primary T helper memory cells from peripheral blood 1 | blood |
4 | chr9:79038000-79046800 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
5 | chr9:79038200-79039400 | Enhancers | Fetal Adrenal Gland | Adrenal Gland |
6 | chr9:79038200-79039600 | Enhancers | Primary T cells from cord blood | blood |
7 | chr9:79038200-79039800 | Enhancers | Primary T helper memory cells from peripheral blood 2 | blood |
8 | chr9:79038400-79039600 | Enhancers | Primary T helper cells fromperipheralblood | blood |
9 | chr9:79038600-79039400 | Enhancers | Primary T helper naive cells from peripheral blood | blood |
10 | chr9:79038800-79039400 | Enhancers | Stomach Mucosa | stomach |
11 | chr9:79039000-79039400 | Enhancers | Primary T helper cells PMA-I stimulated | -- |
12 | chr9:79039000-79039400 | Flanking Active TSS | HepG2 | liver |